Variant #0000681179 (NC_000018.9:g.55816774C>T, NC_000018.9(NM_001144964.1):c.-315-16246C>T (NEDD4L))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55816774C>T
DNA change (hg38) -
Published as NEDD4L(NM_001144968.1):c.7C>T (p.R3C)
ISCN -
DB-ID NEDD4L_000025
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0003 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEDD4L NM_001144964.1 -?/. - c.-315-16246C>T r.(=) p.(=)
NEDD4L NM_001144967.2 -?/. - c.49-16246C>T r.(=) p.(=)


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